[go: up one dir, main page]

US11174247B2 - Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases - Google Patents

Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases Download PDF

Info

Publication number
US11174247B2
US11174247B2 US16/489,227 US201716489227A US11174247B2 US 11174247 B2 US11174247 B2 US 11174247B2 US 201716489227 A US201716489227 A US 201716489227A US 11174247 B2 US11174247 B2 US 11174247B2
Authority
US
United States
Prior art keywords
pharmaceutically acceptable
acceptable salt
aprocitentan
ray powder
powder diffraction
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
US16/489,227
Other languages
English (en)
Other versions
US20200061061A1 (en
Inventor
Marc BELLET
Martin Bolli
Martine Clozel
Marc IGLARZ
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Actelion Pharmaceuticals Ltd
Idorsia Pharmaceuticals Ltd
Original Assignee
Idorsia Pharmaceuticals Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Idorsia Pharmaceuticals Ltd filed Critical Idorsia Pharmaceuticals Ltd
Assigned to IDORSIA PHARMACEUTICALS LTD reassignment IDORSIA PHARMACEUTICALS LTD ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ACTELION PHARMACEUTICALS LTD
Assigned to ACTELION PHARMACEUTICALS LTD reassignment ACTELION PHARMACEUTICALS LTD ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SCHINDELHOLZ, Ivan, BELLET, Marc, BOLLI, MARTIN, CLOZEL, MARTINE, IGLARZ, Marc, KOHLER, Philipp, VON RAUMER, MARKUS
Publication of US20200061061A1 publication Critical patent/US20200061061A1/en
Application granted granted Critical
Publication of US11174247B2 publication Critical patent/US11174247B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/401—Proline; Derivatives thereof, e.g. captopril
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/4035—Isoindoles, e.g. phthalimide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4418—Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4422—1,4-Dihydropyridines, e.g. nifedipine, nicardipine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/549—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame having two or more nitrogen atoms in the same ring, e.g. hydrochlorothiazide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/08—Drugs for disorders of the urinary system of the prostate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A61P27/06—Antiglaucoma agents or miotics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/16—Otologicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Definitions

  • the present invention concerns the compound aprocitentan and its use as endothelin receptor antagonist, in combination with other active ingredients or therapeutic agents including an angiotenin receptor blocker (especially valsartan), and/or a calcium channel blocker (especially amlodipine), and preferably a diuretic which is a thiazide-like diuretic (especially hydrochlorothiazide or chlorthalidone), in the prophylaxis or treatment of certain endothelin related diseases.
  • the invention further relates to pharmaceutical compositions comprising aprocitentan in combination with said other active ingredients or therapeutic agents.
  • the invention further relates to such pharmaceutical compositions comprising novel crystalline forms of aprocitentan; pharmaceutical compositions prepared from such crystalline forms, and to the use of such crystalline forms in combination with said other active ingredients or therapeutic agents in the prophylaxis or treatment of said endothelin related diseases.
  • the compound of formula I also known under the name, and referred to as ACT-132577, is an endothelin receptor inhibitor and useful as endothelin receptor antagonist.
  • the compound of formula I is a member of a structural family that was previously generically disclosed in WO 02/053557.
  • the compound of formula I while showing endothelin receptor antagonist activity, exhibits in vivo a much longer half-life and a much shorter clearance in comparison to corresponding alkylated derivatives. This makes the compound of formula I particularly suitable for long-acting pharmaceutical compositions, as disclosed in WO 2009/024906.
  • the compound of formula I can be used for treatment of endothelin related diseases which are associated with an increase in vasoconstriction, proliferation or inflammation due to endothelin.
  • endothelin related diseases are hypertension, pulmonary hypertension, coronary diseases, cardiac insufficiency, renal and myocardial ischemia, renal failure, cerebral ischemia, dementia, migraine, subarachnoidal hemorrhage, Raynaud's syndrome, digital ulcers and portal hypertension.
  • Atherosclerosis restenosis after balloon or stent angioplasty, inflammation, stomach and duodenal ulcer, cancer, melanoma, prostate cancer, prostatic hypertrophy, erectile dysfunction, hearing loss, amaurosis, chronic bronchitis, asthma, pulmonary fibrosis, gram negative septicemia, shock, sickle cell anemia, glomerulonephritis, renal colic, glaucoma, connective tissue diseases, therapy and prophylaxis of diabetic complications, complications of vascular or cardiac surgery or after organ transplantation, complications of cyclosporin treatment, pain, hyperlipidemia as well as other diseases, presently known to be related to endothelin.
  • hypertension related diseases comprising hypertension including especially difficult to treat/resistant hypertension; pulmonary hypertension; heart failure including especially chronic heart failure; reducing the risk of developing a major cardiovascular event (such as heart failure, myocardial infarction, stroke, or death from cardiovascular causes) in patients who are at cardiovascular risk (such as patients who have coronary artery disease and/or patients who have demonstrated clinical signs of congestive heart failure); angina pectoris; and diastolic dysfunction; erectile dysfunction; CKD (especially CKD of stages 1 to 4 as defined by the Kidney Disease Improving Global Outcomes (KDIGO) Guidelines (and notably CKD of stage 3), and in particular CKD of these stages caused by/associated with essential hypertension, especially resistant hypertension); and diabetes, and diabetes related diseases such as diabetic arteriopathy, diabetic nephropathy, diabetic retinopathy, diabetic vasculopathy; and reducing the risk of developing a major cardiovascular event (such as heart failure, myo
  • resistant hypertension (or difficult to treat hypertension) is defined as uncontrolled blood pressure (BP) (i.e., failure to lower BP to a pre-defined threshold) despite concurrent administration of three antihypertensive therapies of different pharmacological classes at maximal or optimal doses, including a diuretic.
  • BP blood pressure
  • resistant hypertension patients include patients whose blood pressure is controlled with use of more than three medications. That is, patients whose blood pressure is controlled but require four or more medications to do so should be considered resistant to treatment (see e.g. Mancia et al, J. Hypertens . (2013)).
  • ERAs endothelin receptor antagonists
  • therapeutic benefit needs to be weighted against potential side effects, such as the potential risk of teratogenic activity.
  • selective ET A -antagonists and dual antagonists of both the ET A and ET B receptor may cause fluid retention, a common side effect associated with many previously studied ERAs.
  • risk-benefit balance is in most cases in favor of treatment with an ERA for indications such as pulmonary hypertension (as reflected in the past by successive market approvals e.g.
  • ERAs have no role in the management of primary hypertension (Laffin et al. Seminars in Nephrology 2015, 35, 168-175), and side effects such as fluid retention may remain an issue when a potential treatment of rHT, chronic kidney disease or other hypertension related diseases with an ERA is considered.
  • WO2016/073846 provides a comprehensive summary of ERAs tested for various indications including CKD and rHT.
  • ET A -selective ERA avosentan in a trial that investigated the use of avosentan to reduce proteinuria in patients with diabetes, showed significant treatment effect, associated with a significantly increased discontinuation of trial medications due to adverse events, predominantly related to fluid overload and congestive heart failure.
  • the trial was terminated prematurely, and the authors conclude that “it may be that at dosages of 25 to 50 mg, avosentan is less selective for the ETA receptor and thus caused sodium and water retention and peripheral vasodilation with a potential fluid shift from the intravascular to extravascular space.
  • WO2016/073846 concludes in proposing a method of treating CKD with an ERA, especially with the ET A -selective ERA atrasentan, using predictors of fluid retention; said method comprising the determination of a risk of fluid retention if an ERA were administered to the subject; and administering the ERA to the subject if the risk is at an acceptable level.
  • aprocitentan an ERA resulting in effective dual blockade of the endothelin receptors, may result in efficacious control of blood pressure in subjects having essential hypertension, i.e. without background therapy (Actelion Pharmaceuticals Ltd, press release May 22, 2017).
  • the overall frequency of adverse events was similar to those observed in the placebo group.
  • no risk assessment and/or dose reduction to mitigate side effects related to fluid retention may be required for aprocitentan when used in the treatment of hypertension related diseases, especially resistant hypertension.
  • aprocitentan may have synergistic pharmacological effect in combination with valsartan, and synergistic pharmacological effect in combination with amlodipine, compared to the effect of the respective active ingredients alone.
  • three antihypertensive therapies of different pharmacological classes including valsartan, amlodipine, and a diuretic of the thiazide class such as commercially available Exforge HCT® (i.e.
  • aprocitentan may result in superior effect than spironolactone which is a standard available add-on treatment. Moreover, aprocitentan may have a different pharmacological profile than the predominantly ET A -selective antagonists so far tested in resistant hypertension and other endothelin-related diseases.
  • aprocitentan an ERA resulting in effective dual blockade of the endothelin receptors, may be particularly suited for the treatment of resistant hypertension when prescribed in combination with one or more antihypertensive therapies of different pharmacological classes, including especially an angiotensin receptor blocker such as especially valsartan, a calcium channel blocker such as especially amlodipine, and a diuretic, especially a diuretic of the thiazide class (a thiazide-like diuretic) such as especially chlorothiazide, chlorthalidone, hydrochlorothiazide, indapamide, or metolazone.
  • an angiotensin receptor blocker such as especially valsartan
  • a calcium channel blocker such as especially amlodipine
  • a diuretic especially a diuretic of the thiazide class (a thiazide-like diuretic) such as especially chlorothiazide, chlorthalidone,
  • Such combination treatment may result in superior control of blood pressure compared to the treatment with such antihypertensive therapies alone, while maintaining a benign side effect profile even at optimal efficacious dosages of aprocitentan, not requiring e.g. the risk assessment methods of WO2016/073846 and/or dose reductions to mitigate side effects, e.g. related to fluid retention.
  • crystalline forms of aprocitentan that are suitable for the production of pharmaceutical compositions may under certain conditions be found.
  • Said crystalline forms of COMPOUND are novel and may have advantageous properties in view of the potential use of COMPOUND as active pharmaceutical ingredient. Such advantages may include better flow properties; less hygroscopicity; better reproducibiliy in manufacturing (for example better filtration parameters, better reproducibility of formation, and/or better sedimentation); and/or defined morphology.
  • Such crystalline forms of COMPOUND may be particularly suitable in a process of manufacturing certain pharmaceutical compositions. It has also been found that COMPOUND or a pharmaceutically acceptable salt thereof is particularly useful to treat certain disorders, in particular when used in combination with other active ingredients or therapeutic agents.
  • FIG. 1 shows the X-ray powder diffraction diagram of COMPOUND in a crystalline form A as obtained from Example 1.
  • the X-ray diffraction diagram shows peaks having a relative intensity, as compared to the most intense peak in the diagram, of the following percentages (relative peak intensitites given in parenthesis) at the indicated angles of refraction 2theta (selected peaks from the range 3-33° 2theta with relative intensity larger then 10% are reported): 9.8° (18%), 9.9° (18%), 11.7° (14%), 14.5° (10%), 15.4° (14%), 15.6° (29%), 16.9° (19%), 17.2° (16%), 17.8° (100%), 18.6° (50%), 19.9° (54%), 20.0° (67%), 21.5° (24%), 21.9° (10%), 22.8° (18%), 23.2° (49%), 23.5° (83%), 24.9° (32%), 25.1° (20%), 25.3° (24%), 25.6° (33%), 25.9° (16%), 2
  • FIG. 2 shows the X-ray powder diffraction diagram of a dichloromethane solvate of the COMPOUND in a crystalline form B as obtained from Example 2.
  • the X-ray diffraction diagram shows peaks having a relative intensity, as compared to the most intense peak in the diagram, of the following percentages (relative peak intensitites given in parenthesis) at the indicated angles of refraction 2theta (selected peaks from the range 3-33° 2theta with relative intensity larger then 10% are reported): 11.2° (16%), 16.2° (57%), 18.0° (21%), 18.6° (71%), 18.8° (36%), 19.8° (19%), 20.3° (100%), 22.4° (45%), 22.9° (28%), 24.3° (44%), 24.8° (11%), 25.0° (41%), 25.7° (22%), 26.1° (31%), 27.4° (20%), 29.4° (16%), 29.8° (38%) and 32.4° (12%).
  • FIG. 3 shows the X-ray powder diffraction diagram of COMPOUND in a crystalline form C as obtained from Example 3.
  • the X-ray diffraction diagram shows peaks having a relative intensity, as compared to the most intense peak in the diagram, of the following percentages (relative peak intensitites given in parenthesis) at the indicated angles of refraction 2theta (selected peaks from the range 3-33° 2theta with relative intensity larger then 10% are reported): 7.8° (23%), 9.7° (42%), 15.7° (37%), 17.2° (16%), 17.8° (15%), 18.8° (26%), 19.8° (71%), 20.1° (51%), 20.6° (15%), 21.6° (15%), 22.0° (100%), 23.4° (27%), 23.6° (40%), 24.1° (23%), 24.5° (16%), 25.1° (13%), 25.3° (39%), 25.7° (28%), 26.8° (19%), 27.1° (16%), 28.5° (31%), 30.8° (13%) and
  • FIG. 4 shows the X-ray powder diffraction diagram of COMPOUND in a crystalline form D as obtained from Example 4.
  • the X-ray diffraction diagram shows peaks having a relative intensity, as compared to the most intense peak in the diagram, of the following percentages (relative peak intensitites given in parenthesis) at the indicated angles of refraction 2theta (selected peaks from the range 3-33° 2theta with relative intensity larger then 10% are reported): 4.6° (27%), 8.4° (15%), 8.6° (11%), 16.4° (17%), 16.8° (26%), 17.2° (10%), 18.6° (11%), 18.9° (18%), 19.3° (40%), 19.6° (45%), 20.1° (100%), 20.6° (55%), 20.8° (26%), 22.0° (10%), 22.7° (14%), 23.0° (24%), 23.5° (32%), 23.8° (12%), 24.2° (17%), 24.7° (20%), 25.1° (55%), 25.4° (22%), 2
  • FIG. 5 shows the X-ray powder diffraction diagram of an acetonitrile solvate of the COMPOUND in a crystalline form E as obtained from Example 5.
  • the X-ray diffraction diagram shows peaks having a relative intensity, as compared to the most intense peak in the diagram, of the following percentages (relative peak intensitites given in parenthesis) at the indicated angles of refraction 2theta (selected peaks from the range 3-33° 2theta with relative intensity larger then 10% are reported): 9.0° (21%), 9.5° (56%), 11.3° (61%), 14.5° (41%), 14.8° (15%), 15.6° (47%), 16.0° (26%), 16.5° (100%), 18.2° (84%), 18.7° (73%), 18.9° (56%), 20.2° (20%), 20.7° (56%), 22.8° (96%), 23.9° (22%), 24.5° (70%), 25.3° (77%), 25.6° (29%), 26.0° (14%), 26.6° (66%), 27.5
  • FIG. 6 shows the X-ray powder diffraction diagram of COMPOUND in a crystalline form J as obtained from Example 6.
  • the X-ray diffraction diagram shows peaks having a relative intensity, as compared to the most intense peak in the diagram, of the following percentages (relative peak intensitites given in parenthesis) at the indicated angles of refraction 2theta (selected peaks from the range 3-33° 2theta with relative intensity larger then 10% are reported): 4.0° (44%), 4.7° (14%), 6.5° (23%), 9.0° (27%), 16.1° (40%), 17.2° (11%), 18.7° (22%), 19.0° (58%), 19.4° (28%), 19.8° (46%), 20.7° (57%), 21.2° (17%), 21.9° (100%), 22.6° (14%), 23.2° (23%), 24.1° (37%), 24.8° (40%), 25.6° (42%), 27.0° (29%), 28.2° (27%), 29.0° (20%), 30.3° and 30.8
  • FIG. 7 shows the X-ray powder diffraction diagram of a dimethylsulfoxide solvate of the COMPOUND in a crystalline form K as obtained from Example 7.
  • the X-ray diffraction diagram shows peaks having a relative intensity, as compared to the most intense peak in the diagram, of the following percentages (relative peak intensitites given in parenthesis) at the indicated angles of refraction 2theta (selected peaks from the range 3-33° 2theta with relative intensity larger then 10% are reported): 10.9° (16%), 16.9° (18%), 18.2° (26%), 18.4° (30%), 18.6° (29%), 18.7° (55%), 19.3° (100%), 20.8° (35%), 21.2° (47%), 21.9° (26%), 24.3° (21%), 24.8° (24%), 25.4° (29%), 25.8° (22%), 26.7° (34%), 27.7° (13%), 27.8° (14%), 28.6° (15%), 29.4° (18%), 31.5
  • FIG. 8 shows the X-ray powder diffraction diagram of an ethanol solvate of the COMPOUND in a crystalline form L as obtained from Example 8.
  • the X-ray diffraction diagram shows peaks having a relative intensity, as compared to the most intense peak in the diagram, of the following percentages (relative peak intensitites given in parenthesis) at the indicated angles of refraction 2theta (selected peaks from the range 3-33° 2theta with relative intensity larger then 10% are reported): 9.1° (31%), 9.3° (34%), 11.3° (49%), 12.2° (10%), 14.6° (17%), 14.8° (46%), 15.7° (16%), 16.1° (10%), 16.4° (80%), 17.9° (17%), 18.2° (19%), 18.7° (96%), 20.0° (38%), 20.3° (100%), 22.6° (11%), 22.8° (76%), 23.2° (50%), 24.1° (14%), 24.5° (56%), 24.7° (68%), 25.4° (46%),
  • the crystalline forms disclosed herein comprise the COMPOUND in a crystalline form of the free base (i.e. not in form of a salt).
  • said crystalline forms may comprise non-coordinated and/or coordinated solvent. Coordinated solvent is used herein as term for a crystalline solvate.
  • non-coordinated solvent is used herein as term for physiosorbed or physically entrapped solvent (definitions according to Polymorphism in the Pharmaceutical Industry (Ed. R. Hilfiker, VCH, 2006), Chapter 8: U. J. Griesser: The Importance of Solvates).
  • Crystalline forms A and C are anhydrate or ansolvate forms
  • crystalline form B is a DCM solvate
  • crystalline form E is a MeCN solvate
  • crystalline form K is a DMSO solvate.
  • FIG. 9 shows the acute effects of ACT-132577 on mean arterial blood pressure (“MAP”) in conscious, male hypertensive Dahl salt sensitive rats.
  • MAP mean arterial blood pressure
  • FIG. 10 shows the acute effects of ACT-132577 on MAP in conscious, male hypertensive deoxycorticosterone acetate salt rats.
  • FIG. 11 shows the acute effects of ACT-132577 on MAP in conscious, male spontaneously hypertensive rats.
  • FIG. 12 shows the acute effects of ACT-132577, used alone or in combination with valsartan, on MAP in conscious, male spontaneously hypertensive rats.
  • FIG. 13 shows the acute effects of ACT-132577, used alone or in combination with valsartan, on MAP in conscious, male hypertensive deoxycorticosterone acetate salt rats.
  • FIG. 14 shows the acute effects of ACT-132577, used alone or in combination with enalapril, on MAP in conscious, male spontaneously hypertensive rats.
  • FIG. 15 shows the acute effects of ACT-132577, used alone or in combination with amlodipine, on MAP in conscious, male hypertensive deoxycorticosterone acetate salt rats.
  • FIG. 16 shows the effects of chronic oral administration of ACT-132577 on MAP in conscious, male hypertensive deoxycorticosterone acetate salt rats.
  • FIG. 17 shows the effects of chronic oral administration of ACT-132577 on renal vascular resistance in conscious, male hypertensive deoxycorticosterone acetate salt rats.
  • FIG. 18 shows the acute dose-response effect of aprocitentan 1 mg/kg, 3 mg/kg, 10 mg/kg, 30 mg/kg) on haematocrit (Hct) 24 hours after a single oral administration to Wistar rats.
  • FIG. 19 shows acute effects of EXFORGE HCT® alone, and EXFORGE HCT® in combination with ACT-132577, in male spontaneaously hypertensive rats.
  • FIG. 20 shows acute effects of EXFORGE HCT® alone, and EXFORGE HCT® in combination with spironolactone, in male spontaneaously hypertensive rats.
  • FIG. 21 shows acute effects of EXFORGE HCT® alone, and EXFORGE HCT® in combination with ACT-132577, in male hypertensive deoxycorticosterone acetate salt rats.
  • FIG. 22 shows acute effects of EXFORGE HCT® alone, and EXFORGE HCT® in combination with spironolactone, in male hypertensive deoxycorticosterone acetate salt rats.
  • a first embodiment relates to a pharmaceutical composition containing, as active principles, aprocitentan, or a pharmaceutically acceptable salt thereof, in combination with an angiotenin receptor blocker which is especially valsartan, or a pharmaceutically acceptable salt thereof, as well as at least one pharmaceutically acceptable excipient.
  • a second aspect of the present invention relates to a pharmaceutical composition containing, as active principles, aprocitentan, or a pharmaceutically acceptable salt thereof, in combination with
  • aprocitentan is comprised in a pharmaceutical unit dosage form suitable for the oral administration of 12.5 mg or 25 mg per day of aprocitentan
  • valsartan or a pharmaceutically acceptable salt thereof is comprised in a pharmaceutical unit dosage form suitable for the oral administration of 160 mg per day of valsartan
  • amlodipine or a pharmaceutically acceptable salt thereof is comprised in a pharmaceutical unit dosage form suitable for the oral administration of 5 mg or 10 mg per day of amlodipine
  • hydrochlorothiazide or a pharmaceutically acceptable salt thereof is comprised in a pharmaceutical unit dosage form suitable for the oral administration of 12.5 mg or 25 mg per day of hydrochlorothiazide; wherein each dosage combination, i.e.
  • Angiotensin Receptor Blocker in particular means in the present application valsartan, losartan, telmisartan, irbesartan, candesartan, olmesartan, azilsartan, or a pharmaceutically acceptable salt of one of these.
  • a preferred ARB is valsartan or a pharmaceutically acceptable salt thereof.
  • “Calcium Channel Blocker” or “CCB” in particular means in the present application amlodipine, aranidipine, azelnidipine, barnidipine, benidipine, cilnidipine, clevidipine, isradipine, efonidipine, felodipine, lacidipine, lercanidipine, manidipine, nicardipine, nifedipine, nilvadipine, nimodipine, nisoldipine, nitrendipine, pranidipine, verapamil or diltiazem or a pharmaceutically acceptable salt of one of these.
  • a preferred CCB is amlodipine or a pharmaceutically acceptable salt thereof.
  • “Diuretic” in particular means in the present application a diuretic of the thiazide class (a thiazide-like diuretic) such as especially chlorthalidone, hydrochlorothiazide, chlorothiazide, indapamide, or metolazone.
  • Preferred diuretics are chlorthalidone or hydrochlorothiazide; thus one aspect of the present inventions relates to combinations of aprocitentan, the ARB valsartan, and the CCB amlodipine, with chlorthalidone; another aspect of the present invention relates to combinations of aprocitentan, the ARB valsartan, and the CCB amlodipine, with hydrochlorothiazide.
  • compositions containing, as active principles, aprocitentan, or a pharmaceutically acceptable salt thereof, in combination with an Angiotensin Converting Enzyme inhibitor which is especially enalapril, or a pharmaceutically acceptable salt thereof, as well as at least one pharmaceutically acceptable excipient.
  • Angiotensin Converting Enzyme inhibitor or “ACE inhibitor” in particular means in the present application captopril, enalapril, ramipril, quinapril, perindopril, lisinopril, imidapril or cilazapril, or a pharmaceutically acceptable salt of one of these.
  • a preferred ACE inhibitor is enalapril or a pharmaceutically acceptable salt thereof.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form A characterized by the presence of peaks in the X-ray powder diffraction diagram at the following angles of refraction 2 ⁇ : 17.8°, 20.0°, and 23.5°; wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 2 ⁇ values is in the range of 2 ⁇ +/ ⁇ 0.2°.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form A characterized by the presence of peaks in the X-ray powder diffraction diagram at the following angles of refraction 2 ⁇ : 17.8°, 18.6°, 20.0°, 23.2° and 23.5°; wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 2 ⁇ values is in the range of 2 ⁇ +/ ⁇ 0.2°.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form A characterized by the presence of peaks in the X-ray powder diffraction diagram at the following angles of refraction 2 ⁇ : 9.8°, 9.9°, 11.7°, 17.8°, 18.6°, 20.0°, 21.5°, 22.8°, 23.2° and 23.5°; wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 2 ⁇ values is in the range of 2 ⁇ +/ ⁇ 0.2°.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form A characterized by the presence of peaks in the X-ray powder diffraction diagram at the following angles of refraction 2 ⁇ : 9.8°, 9.9°, 11.7°, 14.5°, 15.4°, 15.6°, 16.9°, 17.2°, 17.8°, 18.6°, 19.9°, 20.0°, 21.5°, 21.9°, 22.8°, 23.2°, 23.5°, 24.9°, 25.1°, 25.3°, 25.6°, 25.9°, 27.1°, 27.3°, 28.5°, 29.0°, 29.4°, 30.1° and 30.6°; wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 20 values is in the range of 2 ⁇ +/ ⁇ 0.2°.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form A characterized by the presence of peaks in the X-ray powder diffraction diagram at the following angles of refraction 2 ⁇ : 9.8° (18%), 9.9° (18%), 11.7° (14%), 14.5° (10%), 15.4° (14%), 15.6° (29%), 16.9° (19%), 17.2° (16%), 17.8° (100%), 18.6° (50%), 19.9° (54%), 20.0° (67%), 21.5° (24%), 21.9° (10%), 22.8° (18%), 23.2° (49%), 23.5° (83%), 24.9° (32%), 25.1° (20%), 25.3° (24%), 25.6° (33%), 25.9° (16%), 27.1° (23%), 27.3° (39%), 28.5° (13%), 29.0° (23%), 29.4° (15%), 30.1° (12%) and 30.6° (10%); wherein said X-ray powder
  • the present data show peaks having a relative intensity, as compared to the most intense peak in the diagram, of the following percentages (relative peak intensitites given in parentheses) at the indicated angles of refraction 2theta (selected peaks from the range 3-33° 2theta with relative intensity larger then 10% are reported).
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form A which essentially shows the X-ray powder diffraction pattern as depicted in FIG. 1 , wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 2 ⁇ values is in the range of 2 ⁇ +/ ⁇ 0.2°.
  • the term “essentially” means that at least the major peaks of the diagram depicted in said figures, i.e. those having a relative intensity of more than 10%, especially more than 20%, as compared to the most intense peak in the diagram, have to be present.
  • the person skilled in the art of X-ray powder diffraction will recognize that relative intensities in X-ray powder diffraction diagrams may be subject to strong intensity variations due to preferred orientation effects.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form A obtainable by crystallisation of the COMPOUND in an aqueous solution at pH 6.2 to 6.8.
  • the 2 ⁇ value given is to be understood as an interval from said value minus 0.2° to said value plus 0.2° (2 ⁇ +/ ⁇ 0.2°); and preferably from said value minus 0.1 to said value plus 0.1 (2 ⁇ +/ ⁇ 0.1).
  • n equivalent(s) is used wherein n is a number, it is meant and within the scope of the current application that n is referring to about the number n, preferably n is referring to the exact number n.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form C characterized by the presence of peaks in the X-ray powder diffraction diagram at the following angles of refraction 2 ⁇ : 9.7°, 15.7°, and 22.0°; wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 2 ⁇ values is in the range of 2 ⁇ +/ ⁇ 0.2°.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form C characterized by the presence of peaks in the X-ray powder diffraction diagram at the following angles of refraction 2 ⁇ : 7.8°, 9.7°, 15.7°, 19.8° and 22.0°; wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 2 ⁇ values is in the range of 2 ⁇ +/ ⁇ 0.2°.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form C characterized by the presence of peaks in the X-ray powder diffraction diagram at the following angles of refraction 2 ⁇ : 7.8°, 9.7°, 15.7°, 17.2°, 17.8°, 18.8°, 19.8°, 22.0°, 23.6°, and 25.3°; wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 2 ⁇ values is in the range of 2 ⁇ +/ ⁇ 0.2°.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form C characterized by the presence of peaks in the X-ray powder diffraction diagram at the following angles of refraction 2 ⁇ : 7.8°, 9.7°, 15.7°, 17.2°, 17.8°, 18.8°, 19.8°, 20.1°, 20.6°, 21.6°, 22.0°, 23.4°, 23.6°, 24.1°, 24.5°, 25.1°, 25.3°, 25.7°, 26.8°, 27.1°, 28.5°, 30.8° and 30.8°; wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 2 ⁇ values is in the range of 2 ⁇ +/ ⁇ 0.2°.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form C characterized by the presence of peaks in the X-ray powder diffraction diagram at the following angles of refraction 2 ⁇ : 7.8° (23%), 9.7° (42%), 15.7° (37%), 17.2° (16%), 17.8° (15%), 18.8° (26%), 19.8° (71%), 20.1° (51%), 20.6° (15%), 21.6° (15%), 22.0° (100%), 23.4° (27%), 23.6° (40%), 24.1° (23%), 24.5° (16%), 25.1° (13%), 25.3° (39%), 25.7° (28%), 26.8° (19%), 27.1° (16%), 28.5° (31%), 30.8° (13%) and 30.8° (13%); wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 2 ⁇ values is in
  • the present data show peaks having a relative intensity, as compared to the most intense peak in the diagram, of the following percentages (relative peak intensitites given in parentheses) at the indicated angles of refraction 2theta (selected peaks from the range 3-33° 2theta with relative intensity larger then 10% are reported).
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form C which essentially shows the X-ray powder diffraction pattern as depicted in FIG. 3 , wherein said X-ray powder diffraction diagram is obtained by using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping; and the accuracy of the 2 ⁇ values is in the range of 2 ⁇ +/ ⁇ 0.2°.
  • the term “essentially” means that at least the major peaks of the diagram depicted in said figures, i.e. those having a relative intensity of more than 10%, especially more than 20%, as compared to the most intense peak in the diagram, have to be present.
  • the person skilled in the art of X-ray powder diffraction will recognize that relative intensities in X-ray powder diffraction diagrams may be subject to strong intensity variations due to preferred orientation effects.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in crystalline Form C obtainable by crystallisation of the COMPOUND from MeOH, EtOH or propan-2-ol.
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 7), said composition comprising aprocitentan in amorphous form.
  • amorphous form may be obtained by milling form A.
  • the amorphous form is obtainable by milling in a ball mill (MM200 Retsch Ball Mill, 2 agate beads), 30 min at 30 Hz at ambient temperature.
  • compositions can be effected in a manner which will be familiar to any person skilled in the art (see for example Remington, The Science and Practice of Pharmacy, 21st Edition (2005), Part 5, “Pharmaceutical Manufacturing” [published by Lippincott Williams & Wilkins]) by bringing the crystalline forms of the present invention, optionally in combination with other therapeutically valuable substances, into a galenical administration form together with suitable, non-toxic, inert, pharmaceutically acceptable solid or liquid carrier materials and, if desired, usual pharmaceutical adjuvants.
  • a further embodiment relates to a solid pharmaceutical composition (in particular in the form of a tablet) according to any one of embodiments 1) to 22), especially according to any one of embodiments 8) to 14), or according to any one of embodiments 15) to 21), comprising as pharmaceutically acceptable excipient inert microcrystalline cellulose, lactose, hydroxypropylcellulose, croscarmellose sodium and magnesium stearate.
  • the solid pharmaceutical composition of embodiment 23) will comprise aprocitentan in a total amount from 5 to 25% in weight based on the total weight of the pharmaceutical composition, microcrystalline cellulose in a total amount from 20 to 30% in weight based on the total weight of the pharmaceutical composition, lactose in a total amount from 40 to 65% in weight based on the total weight of the pharmaceutical composition, hydroxypropylcellulose in a total amount from 1 to 3% in weight based on the total weight of the pharmaceutical composition, croscarmellose sodium in a total amount from 2 to 8% in weight based on the total weight of the pharmaceutical composition and magnesium stearate in a total amount from 0.2 to 2% in weight based on the total weight of the pharmaceutical composition, whereby the total percent in weight of the solid pharmaceutical composition will always be 100; the aforementioned solid pharmaceutical composition will particularly be in the form of a tablet.
  • a further embodiment of the invention relates to a pharmaceutical composition according to embodiments 23) to 24), wherein said pharmaceutical composition is in form of a tablet.
  • the pharmaceutically active ingredients are comprised in granules prior to compression to said tablet.
  • a tablet according to embodiment 25 can optionally be coated with a suitable protective pellicle.
  • Said protective pellicle will notably prevent direct contact of the pharmaceutical composition with moisture; it may also ease imprints that may be desired to be used in order to distinguish the pharmaceutical composition from others.
  • the coating material for making such protective pellicle may include a low water vapour permeability polymer (such as a polyvinyl alcohol (e.g. Aquapolish® white PVA from manufacturer Biogrund) or dimethylaminoethyl methacrylate (e.g. EUDRAGIT® E PO)).
  • the coating material can further include a plasticizing agent (e.g. propylene glycol, triacetyne, dibutyl phthalate or dibutyl sebacate), a surfactant (e.g. sodium lauryl sulphate or a polysorbate such as Tween®) and/or a lubricant/glidant (e.g. stearic acid, magnesium or calcium stearate or talc).
  • the coating material can also include a pigment (e.g. iron(II) oxide, iron(III) oxide or titanium oxide) to give the tablet a coloured aspect.
  • a further embodiment of the invention relates to a pharmaceutical composition according to any one of embodiments 23) to 24), wherein said pharmaceutical composition is in form of a capsule.
  • the pharmaceutically active ingredients are comprised in granules prior to filling into said capsules.
  • the invention further relates to the crystalline forms of aprocitentan, especially to crystalline form A, disclosed herein wherein such crystalline form is suitable/is used as final isolation step of aprocitentan (e.g. in order to meet the purity requirements of pharmaceutical production), whereas the final pharmaceutical composition according to embodiments 1 to 26) may or may not contain said crystalline form (e.g. because the originally crystalline form of aprocitentan is further transformed during the manufacturing process and/or is dissolved in the pharmaceutically acceptable carrier material(s); thus, in the final pharmaceutical composition, aprocitentan may be present in non-crystalline form, in another crystalline form, or in dissolved form, or the like).
  • Such combination pharmaceutical compositions according to embodiments 1) to 26) are especially useful for the treatment of endothelin related diseases including hypertension, pulmonary hypertension, coronary diseases, cardiac insufficiency, renal and myocardial ischemia, renal failure, cerebral ischemia, dementia, migraine, subarachnoidal hemorrhage, Raynaud's syndrome, digital ulcers or portal hypertension as well as for the treatment or prevention of atherosclerosis, restenosis after balloon or stent angioplasty, inflammation, stomach and duodenal ulcer, cancer, melanoma, prostate cancer, prostatic hypertrophy, erectile dysfunction, hearing loss, amaurosis, chronic bronchitis, asthma, pulmonary fibrosis, gram negative septicemia, shock, sickle cell anemia, glomerulonephritis, renal colic, glaucoma, connective tissue diseases, diabetic complications, complications of vascular or cardiac surgery or after organ transplantation, complications of cyclosporin treatment, pain or hyperlipidemia.
  • the combination pharmaceutical compositions according to embodiments 1) to 26) are also useful for the treatment of Chronic Kidney Disease (CKD), especially CKD of stages 1 to 4 as defined by the Kidney Disease Improving Global Outcomes (KDIGO) Guidelines (and notably CKD of stage 3), and in particular CKD of these stages caused by essential hypertension.
  • CKD Chronic Kidney Disease
  • KDIGO Kidney Disease Improving Global Outcomes
  • compositions according to embodiments 1) to 26) are especially useful for the treatment of hypertension related diseases comprising hypertension including especially difficult to treat/resistant hypertension; pulmonary hypertension; heart failure including especially chronic heart failure; reducing the risk of developing a major cardiovascular event (such as heart failure, myocardial infarction, stroke, or death from cardiovascular causes) in patients who are at cardiovascular risk (such as patients who have coronary artery disease and/or patients who have demonstrated clinical signs of congestive heart failure); angina pectoris; and diastolic dysfunction; erectile dysfunction; CKD (especially CKD of stages 1 to 4 as defined by the Kidney Disease Improving Global Outcomes (KDIGO) Guidelines (and notably CKD of stage 3), and in particular CKD of these stages caused by/associated with essential hypertension, especially resistant hypertension); and diabetes, and diabetes related diseases such as diabetic arteriopathy, diabetic nephropathy, diabetic retinopathy, diabetic vasculopathy; and reducing the risk of developing a major cardiovascular event
  • the pharmaceutical compositions according to embodiments 1) to 26) are useful for in the treatment of certain endothelin related diseases, which may be defined as a disease selected from the group consisting of hypertension, pulmonary hypertension, diabetic arteriopathy, heart failure, erectile dysfunction, angina pectoris and CKD (especially CKD of stages 1 to 4 as defined by the Kidney Disease Improving Global Outcomes (KDIGO) Guidelines (and notably CKD of stage 3), and in particular CKD of these stages caused by essential hypertension).
  • endothelin related diseases which may be defined as a disease selected from the group consisting of hypertension, pulmonary hypertension, diabetic arteriopathy, heart failure, erectile dysfunction, angina pectoris and CKD (especially CKD of stages 1 to 4 as defined by the Kidney Disease Improving Global Outcomes (KDIGO) Guidelines (and notably CKD of stage 3), and in particular CKD of these stages caused by essential hypertension).
  • compositions according to embodiments 1) to 19) are useful in the treatment of a disease selected from the group consisting of essential hypertension, resistant hypertension, pulmonary hypertension and pulmonary arterial hypertension (and notably in the treatment of resistant hypertension).
  • Essential hypertension also called primary hypertension or idiopathic hypertension
  • the diagnosis of essential hypertension is made when the average of multiple systolic blood pressure measurements on 2 or more subsequent visits is consistently equal to or above a certain threshold value T SBP .
  • T SBP threshold value
  • Individuals with high normal blood pressure tend to maintain pressures that are above average for the general population and are at greater risk for development of definite hypertension and cardiovascular events than the general population.
  • the threshold value T SBP above which treatment is recommended is regularly discussed among clinicians (see e.g. Mancia et al, J. Hypertens . (2013), 31, 1281-1357); accordingly, depending on the patient's general condition and age, T SBP could be 140 or 130 mm Hg, or another suitable value.
  • resistant hypertension [equivalent to the term “difficult to treat hypertension” ] in the present invention is defined as blood pressure that remains above goal in spite of the concurrent use of 3 antihypertensive agents of different classes.
  • One of the 3 agents should be a diuretic and all agents should be prescribed at optimal/maximal dose amounts.
  • resistant hypertension patients include patients whose blood pressure is controlled with use of more than 3 medications. That is, patients whose blood pressure is controlled but require 4 or more medications to do so should be considered resistant to treatment (see e.g. Mancia et al, J. Hypertens . (2013), 31, 1281-1357).
  • a fourth aspect of the invention thus relates to aprocitentan, or a pharmaceutically acceptable salt thereof, for use in the treatment of hypertension, pulmonary hypertension, diabetic arteriopathy, heart failure, erectile dysfunction, angina pectoris and chronic kidney disease (notably in the treatment of resistant hypertension), wherein aprocitentan is to be administered in combination with an angiotenin receptor blocker which is especially valsartan, or a pharmaceutically acceptable salt thereof.
  • a further embodiment relates to aprocitentan, or a pharmaceutically acceptable salt thereof, for use in the treatment of hypertension, pulmonary hypertension, diabetic arteriopathy, heart failure, erectile dysfunction, angina pectoris and chronic kidney disease (notably in the treatment of resistant hypertension), wherein aprocitentan is to be administered in combination with
  • aprocitentan or a pharmaceutically acceptable salt thereof is for use in combination with said further pharmaceutically active ingredients.
  • the corresponding combined treatment may be effected simultaneously, separately, or over a period of time (especially simultaneously).
  • “Simultaneously”, when referring to an administration type, means in the present application that the administration type concerned consists in the administration of two or more active ingredients and/or treatments at approximately the same time; wherein it is understood that a simultaneous administration will lead to exposure of the subject to the two or more active ingredients and/or treatments at the same time.
  • said two or more active ingredients may be administered in a fixed dose combination, or in an equivalent non-fixed dose combination (e.g. by using two or more different pharmaceutical compositions to be administered by the same route of administration at approximately the same time), or by a non-fixed dose combination using two or more different routes of administration; wherein said administration leads to essentially simultaneous exposure of the subject to the two or more active ingredients and/or treatments.
  • the COMPOUND would possibly be used “simultaneously”.
  • “Fixed dose combination”, when referring to an administration type, means in the present application that the administration type concerned consists in the administration of one single pharmaceutical composition comprising the two or more active ingredients, such as especially the pharmaceutical compositions of embodiments 1) to 26).
  • “Separately”, when referring to an administration type, means in the present application that the administration type concerned consists in the administration of two or more active ingredients and/or treatments at different points in time; wherein it is understood that a separate administration will lead to a treatment phase (e.g. at least 1 hour, notably at least 6 hours, especially at least 12 hours) where the subject is exposed to the two or more active ingredients and/or treatments at the same time; but a separate administration may also lead to a treatment phase where for a certain period of time (e.g. at least 12 hours, especially at least one day) the subject is exposed to only one of the two or more active ingredients and/or treatments.
  • a treatment phase e.g. at least 1 hour, notably at least 6 hours, especially at least 12 hours
  • a separate administration may also lead to a treatment phase where for a certain period of time (e.g. at least 12 hours, especially at least one day) the subject is exposed to only one of the two or more active ingredients and/or treatments.
  • Separate administration especially refers to situations wherein at least one of the active ingredients and/or treatments is given with a periodicity substantially different from daily (such as once or twice daily) administration (e.g. wherein one active ingredient and/or treatment is given e.g. once or twice a day, and another is given e.g. every other day, or once a week or at even longer distances).
  • administration “over a period of time” is meant in the present application the subsequent administration of two or more active ingredients and/or treatments at different times.
  • the term in particular refers to an administration method according to which the entire administration of one of the active ingredients and/or treatments is completed before the administration of the other/the others begins. In this way it is possible to administer one of the active ingredients and/or treatments for several months before administering the other active ingredient(s) and/or treatment(s).
  • a further embodiment relates to a pharmaceutical composition according to any one of embodiments 1) to 26) for use in the treatment of hypertension including resistant hypertension; heart failure including chronic heart failure; diastolic dysfunction; CKD including CKD of stage 3 caused by or associated with essential hypertension; or for the reduction of the risk of developing a major cardiovascular event in patients who have diabetes that is accompanied by at least one other cardiovascular risk factor comprising hypertension.
  • aprocitentan or a pharmaceutically acceptable salt thereof, for use in the treatment of certain endothelin related diseases, wherein aprocitentan is to be administered in combination with further active ingredients such as:
  • X-ray powder diffraction patterns were collected on a Bruker D8 Advance X-ray diffractometer equipped with a Lynxeye detector operated with CuK ⁇ -radiation in reflection mode (coupled two Theta/Theta). Typically, the X-ray tube was run at of 40 kV/40 mA. A step size of 0.02° (26) and a step time of 76.8 sec over a scanning range of 3-50° in 26 were applied. The divergence slit was set to fixed 0.3. Powders were slightly pressed into a silicon single crystal sample holder with depth of 0.5 mm and samples were rotated in their own plane during the measurement.
  • Diffraction data are reported using combined Cu K ⁇ 1 and K ⁇ 2 radiation, without K ⁇ 2 stripping.
  • the accuracy of the 2 ⁇ values as provided herein is in the range of +/ ⁇ 0.1-0.2° as it is generally the case for conventionally recorded X-ray powder diffraction patterns.
  • the aq. phase was washed a second time with EtOAc/iPrOAc 1:1 (500 mL, 5 vol.).
  • 1M H 2 SO 4 200 mL, 0.2 mol, 1 eq., 2 vol.
  • Crystallization started at pH 8.5-8.0.
  • the crude product was filtered off as XRPD pattern form K (DMSO solvate) or a mixture of form A and form K. It was washed twice with water (2 ⁇ 1000 mL, 2 ⁇ 10 vol.). The solid was slurried in water (1000 mL, 10 vol.) at rt for 3 h.
  • Tablets containing each 50 mg of ACT-132577 can be prepared using a wet granulation process.
  • the tablet composition is the following:
  • ACT-132577 tablets 250 mg
  • Microcrystalline cellulose 61.50 24.60 Lactose (200M) 122.25 48.90 Hydroxypropylcellulose 5.50 2.20 Croscarmellose sodium 4.50 1.80 Water qs qs Extra- Croscarmellose sodium 5.00 2.00 granular Magnesium stearate 1.25 0.50 Total 250.00 100.00 qs quantity sufficient
  • ACT-132577 Form A (as described herein) will be used for making the tablets.
  • Example 9 The tablets of Example 9 can be coated with a layer of Aquapolish® white MS or Aquapolish® white PVA (coating manufacturer: Bioground).
  • Tablets containing each 50 mg of ACT-132577 can be prepared using a wet granulation process.
  • the tablet composition is the following:
  • ACT-132577 tablets 250 mg
  • Microcrystalline cellulose 61.25 24.50 Lactose (200M) 122.50 49.00 Hydroxypropylcellulose 5.00 2.00 Croscarmellose sodium 5.00 2.00 Water qs qs Extra- Croscarmellose sodium 5.00 2.00 granular Magnesium stearate 1.25 0.50 Total 250.00 100.00 qs quantity sufficient
  • ACT-132577 Form A (as described herein) will be used for making the tablets.
  • Example 11 can be coated with a layer of Aquapolish® white MS or Aquapolish® white PVA (coating manufacturer: Bioground).
  • Tablets containing each 12.5 mg of ACT-132577 can be prepared using a wet granulation process.
  • the tablet composition is the following:
  • ACT-132577 tablets 100 mg
  • Material (Chemical name) mg/tablet Weight %/tablet Intra- ACT-132577 (amorphous, solid 12.50 12.50 granular form A or solid form C, as described herein)
  • Microcrystalline cellulose 27.00 27.00 Lactose (200M) 54.00 54.00 Hydroxypropylcellulose 2.00 2.00 Croscarmellose sodium 2.00 2.00 Water qs qs Extra- Croscarmellose sodium 2.00 2.00 granular Magnesium stearate 0.50 0.50 Total 100.00 100.00 qs quantity sufficient
  • ACT-132577 Form A (as described herein) will be used for making the tablets.
  • Example 13 The tablets of Example 13 can be coated with a layer of Aquapolish® white MS or Aquapolish® white PVA (coating manufacturer: Bioground).
  • Tablets containing each 12.5 mg of ACT-132577 can be prepared using a wet granulation process.
  • the tablet composition is the following:
  • ACT-132577 tablets 100 mg
  • MATERIAL CHEMICAL NAME
  • mg/tablet Weight %/tablet Intra- ACT-132577 amorphous, solid 12.50 12.50 granular form A or solid form C, as described herein
  • Microcrystalline cellulose 27.50 27.50 Lactose (200M) 53.50 53.50 Hydroxypropylcellulose 2.20 2.20 Croscarmellose sodium 1.80 1.80 Water qs qs Extra- Croscarmellose sodium 2.00 2.00 granular Magnesium stearate 0.50 0.50 Total 100.00 100.00 qs quantity sufficient
  • ACT-132577 Form A (as described herein) will be used for making the tablets.
  • Example 15 can be coated with a layer of Aquapolish® white MS or Aquapolish® white PVA (coating manufacturer: Bioground).
  • a sample of Form A crystals of the COMPOUND (as obtained according to Example 1 above) has been stored at a temperature of 20-25° C. at 92% relative humidity for 2 months. X-ray powder diffraction performed on that sample at the end of the 2 months showed that the sample was still consisting only in Form A crystals of the COMPOUND. The same result was obtained after storage for 8 weeks under the above conditions. HPLC control of the sample after 8 weeks storage revealed no significant change in peak area %, i.e. no significant degradation was observed under such conditions.
  • a sample of Form B crystals of a dichloromethane solvate of the COMPOUND (as obtained according to Example 2 above) has been stored in a closed vial (20 mg of Form B crystals being placed in a closed 4 mL vial) at a temperature of 20-25° C. for about 3 weeks. X-ray powder diffraction performed on that sample at the end of the 3 weeks showed that the Form B crystals were transformed into Form A crystals of the COMPOUND.
  • a sample of Form K crystals of a dimethylsulfoxide solvate of the COMPOUND (as obtained according to Example 7 above) has been stored in a closed vial (20 mg of Form K crystals being placed in a closed 4 mL vial) at a temperature of 20-25° C. for about 3 weeks. X-ray powder diffraction performed on that sample at the end of the 3 weeks showed that the Form K crystals were transformed into Form A crystals of the COMPOUND.
  • Form A is considered to be slightly hygroscopic as determined by gravimetric vapor sorption (GVS). Mass increase of a sample as obtained according to Example 1 in the first cycle from 40% r.h. to 80% r.h. corresponds to 0.4%. At 95% r.h. 2.2% moisture were taken up in a reversible way without hysteresis upon drying.
  • VGS gravimetric vapor sorption
  • MAP mean arterial blood pressure
  • HR heart rate
  • Elevated blood pressure is induced in Dahl-S rats by providing 1% sodium chloride in drinking water.
  • Groups of 6-7 Dahl-S rats were used for the vehicle (7.5% gelatin aquous solution) and each dose of ACT-132577 tested (0.3, 1, 3, 10, 30, 100, and 300 mg/kg).
  • Effects of ACT-132577 on HR and MAP were calculated for individual animals relative to the 24 h period before administering.
  • the results obtained regarding MAP are summarised in FIG. 9 (data are presented as mean ⁇ standard error of the mean).
  • a dose of 10 mg/kg ACT-132577 decreased MAP by 19 ⁇ 4 mm Hg in Dahl-S rats.
  • HR was not affected.
  • MAP mean arterial blood pressure
  • HR heart rate
  • MAP mean arterial blood pressure
  • HR heart rate
  • ACT-132577 administered orally at a single dose of 100 mg/kg on blood pressure, in particular on mean arterial blood pressure (hereafter “MAP”), and heart rate (hereafter “HR”), with ACT-132577 being used either alone or in combination with valsartan administered orally at a single dose of 10 mg/kg, were evaluated by means of telemetry in conscious, male spontaneaously hypertensive rats (hereafter “SHRs”—see details about this model in Atanur et al., Genome Res . (2010), 20, 791-803).
  • SHRs mean arterial blood pressure
  • ACT-132577 administered orally at a single dose of 10 mg/kg on blood pressure, in particular on mean arterial blood pressure (hereafter “MAP”), and heart rate (hereafter “HR”), with ACT-132577 being used either alone or in combination with valsartan administered orally at a single dose of 30 mg/kg, were evaluated by means of telemetry in conscious, male hypertensive deoxycorticosterone acetate salt rats (hereafter “DOCA-salt rats”—see details about this model in Gavras et al., Circ. Res. (1975), 36, 300-309).
  • MAP mean arterial blood pressure
  • HR heart rate
  • ACT-132577 administered orally at a single dose of 100 mg/kg on blood pressure, in particular on mean arterial blood pressure (hereafter “MAP”), and heart rate (hereafter “HR”), with ACT-132577 being used either alone or in combination with enalapril administered orally at a single dose of 3 mg/kg, were evaluated by means of telemetry in conscious, male spontaneaously hypertensive rats (hereafter “SHRs”—see details about this model in Atanur et al., Genome Res . (2010), 20, 791-803).
  • SHRs mean arterial blood pressure
  • ACT-132577 administered orally at a single dose of 10 mg/kg on blood pressure, in particular on mean arterial blood pressure (hereafter “MAP”), and heart rate (hereafter “HR”), with ACT-132577 being used either alone or in combination with amlodipine administered orally at a single dose of 1 mg/kg, were evaluated by means of telemetry in conscious, male hypertensive deoxycorticosterone acetate salt rats (hereafter “DOCA-salt rats”—see details about this model in Gavras et al., Circ. Res. (1975), 36, 300-309).
  • MAP mean arterial blood pressure
  • HR heart rate
  • ACT-132577 The chronic effects of repeated administrations of doses of 1, 10 and 100 mg/kg/day of ACT-132577, in particular mean arterial blood pressure (hereafter “MAP”), and heart rate (hereafter “HR”), were evaluated in conscious, male hypertensive deoxycorticosterone acetate salt rats (hereafter “DOCA-salt rats”—see details about this model in Gavras et al., Circ. Res. (1975), 36, 300-309).
  • DOCA-salt rats hypertension is induced by the combination of unilateral nephrectomy, implantation of pellets of the mineralocorticoid analog DOCA, and provision of 1% sodium chloride in drinking water.
  • the results of the DOCA-salt rats treated with ACT-132577 were compared to those obtained for Wistar rats or for DOCA-salt rats that received only the vehicle (4% gelatin aquous solution).
  • ACT-132577 chronic oral administration of ACT-132577 to DOCA-salt rats dose-dependently increased renal blood flow and decreased renal vascular resistance.
  • ACT-132577 also tended to decrease left ventricular hypertrophy, as suggested by the dose-dependent decrease in plasma concentrations of N-terminal pro-brain natriuretic peptide (NTproBNP).
  • NproBNP N-terminal pro-brain natriuretic peptide
  • ACT-132577 can be assessed in diabetic rodent models (in this regard, see the models described in the following references: Sen et al, Life Sci . (2012), 91(13-14), 658-668; Janiak et al., Eur. J. Pharmacol . (2006), 534, 271-279; and Iglarz et al, J. Pharmacol. Exp. Ther . (2008), 327(3), 736-745).
  • End organ damage includes: vascular function, renal function (e.g. proteinuria), cardiac function and remodelling and any other target organ affected by diabetes (e.g. the eye).
  • haematocrit haemoglobin occurs secondary to an increase in plasma volume and can be used as a marker of fluid retention.
  • a single oral dose of aprocitentan (1-30 mg/kg) or vehicle (gelatin) was administered by gavage to male Wistar rats. Twenty-four hours after administration, sublingual blood was sampled under isoflurane-induced anesthesia. Haematocrit was measured using a hematology analyser. ACT-132577 did not impact on haematocrit (Hct) suggesting low liability on fluid retention ( FIG. 18 ).
  • MAP mean arterial blood pressure
  • HR heart rate
  • Exforge HCT® i.e. a fixed dose combination of valsartan/amlodipine/hydrochlorothiazide; dosage adapted for 1.6 mg/kg/0.1 mg/kg/0.25 mg/kg for valsartan/amlodipine/hydrochlorothiazide, respectively
  • MAP mean arterial blood pressure
  • HR heart rate
  • Exforge HCT® (dosage adapted for 3.2 mg/kg/0.2 mg/kg/0.5 mg/kg for valsartan/amlodipine/hydrochlorothiazide, respectively) on blood pressure, in particular on mean arterial blood pressure (hereafter “MAP”), and heart rate (hereafter “HR”) in combination with ACT-132577 (10 mg/kg) or spironolactone (300 mg/kg), each administered orally as single doses, were also evaluated by means of telemetry in conscious, male hypertensive deoxycorticosterone acetate salt rats (hereafter “DOCA-salt rats”-see details about this model in Gavras et al., Circ. Res. (1975), 36, 300-309).
  • MAP mean arterial blood pressure
  • HR heart rate
  • ACT-132577 10 mg/kg
  • spironolactone 300 mg/kg
  • DOCA-salt rats hypertension is induced by the combination of unilateral nephrectomy, implantation of pellets of the mineralocorticoid analog DOCA, and provision of 1% sodium chloride in drinking water. 7-9 DOCA-salt rats per treatment group were used for this test.
  • the results obtained regarding MAP are summarised in FIGS. 21 and 22 wherein each data point is presented as a 6-hour mean.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Pulmonology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Hospice & Palliative Care (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Gynecology & Obstetrics (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Vascular Medicine (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicinal Preparation (AREA)
  • Nutrition Science (AREA)
  • Physiology (AREA)
US16/489,227 2017-02-27 2017-11-06 Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases Active US11174247B2 (en)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
EP2017054489 2017-02-27
EPPCT/EP2017/054489 2017-02-27
WOPCT/EP2017/054489 2017-02-27
WOPCT/EP2017/061487 2017-05-12
EP2017061487 2017-05-12
EPPCT/EP2017/061487 2017-05-12
PCT/EP2017/078371 WO2018153513A1 (en) 2017-02-27 2017-11-06 Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2017/078371 A-371-Of-International WO2018153513A1 (en) 2017-02-27 2017-11-06 Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US17/472,349 Continuation US11787782B2 (en) 2017-02-27 2021-09-10 Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases

Publications (2)

Publication Number Publication Date
US20200061061A1 US20200061061A1 (en) 2020-02-27
US11174247B2 true US11174247B2 (en) 2021-11-16

Family

ID=60268369

Family Applications (5)

Application Number Title Priority Date Filing Date
US16/489,227 Active US11174247B2 (en) 2017-02-27 2017-11-06 Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases
US16/489,194 Active US10919881B2 (en) 2017-02-27 2018-02-26 Crystalline forms of a 4-pyrimidinesulfamide derivative aprocitentan
US17/146,801 Active 2038-07-26 US11680058B2 (en) 2017-02-27 2021-01-12 Crystalline forms of a 4-pyrimidinesulfamide derivative aprocitentan
US17/472,349 Active 2038-03-02 US11787782B2 (en) 2017-02-27 2021-09-10 Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases
US18/319,402 Pending US20230391757A1 (en) 2017-02-27 2023-05-17 Crystalline forms of a 4-pyrimidinesulfamide derivative aprocitentan

Family Applications After (4)

Application Number Title Priority Date Filing Date
US16/489,194 Active US10919881B2 (en) 2017-02-27 2018-02-26 Crystalline forms of a 4-pyrimidinesulfamide derivative aprocitentan
US17/146,801 Active 2038-07-26 US11680058B2 (en) 2017-02-27 2021-01-12 Crystalline forms of a 4-pyrimidinesulfamide derivative aprocitentan
US17/472,349 Active 2038-03-02 US11787782B2 (en) 2017-02-27 2021-09-10 Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases
US18/319,402 Pending US20230391757A1 (en) 2017-02-27 2023-05-17 Crystalline forms of a 4-pyrimidinesulfamide derivative aprocitentan

Country Status (28)

Country Link
US (5) US11174247B2 (ko)
EP (3) EP3658140A1 (ko)
JP (3) JP7223701B2 (ko)
KR (3) KR102700778B1 (ko)
CN (3) CN110325186A (ko)
AU (2) AU2017400276B2 (ko)
BR (2) BR112019017658A2 (ko)
CA (2) CA3053991A1 (ko)
CL (3) CL2019002464A1 (ko)
DK (1) DK4014976T3 (ko)
ES (1) ES3006308T3 (ko)
FI (1) FI4014976T3 (ko)
HR (1) HRP20241461T1 (ko)
HU (1) HUE069231T2 (ko)
IL (4) IL268850B2 (ko)
LT (1) LT4014976T (ko)
MA (2) MA49664A (ko)
MX (3) MX392313B (ko)
MY (1) MY199557A (ko)
PH (2) PH12019501938A1 (ko)
PL (1) PL4014976T3 (ko)
PT (1) PT4014976T (ko)
RS (1) RS66200B1 (ko)
SG (3) SG11201907435PA (ko)
SI (1) SI4014976T1 (ko)
TW (2) TWI854353B (ko)
UA (1) UA126122C2 (ko)
WO (2) WO2018153513A1 (ko)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11464777B2 (en) 2018-12-21 2022-10-11 Actelion Pharmaceuticals Ltd Pharmaceutical composition for the treatment of pulmonary arterial hypertension
US11612600B2 (en) 2019-01-25 2023-03-28 Actelion Pharmaceuticals Ltd Pharmaceutical composition comprising macitentan for the treatment of chronic thromboembolic pulmonary hypertension
US11680058B2 (en) 2017-02-27 2023-06-20 Idorsia Pharmaceuticals Ltd Crystalline forms of a 4-pyrimidinesulfamide derivative aprocitentan
US12144811B2 (en) 2017-11-30 2024-11-19 Idorsia Pharmaceuticals Ltd Combination of a 4-pyrimidinesulfamide derivative with an SGLT-2 inhibitor for the treatment of endothelin related diseases

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2958110A1 (en) * 2014-08-14 2016-02-18 Vivus, Inc. Treatment of sleep apnea with a combination of a carbonic anhydrase inhibitor and an aldosterone antagonist
JP7312262B2 (ja) 2018-09-28 2023-07-20 フロー メディカル コーポレイション カテーテル装置
CN112569357B (zh) * 2019-09-30 2023-03-28 深圳奥萨制药有限公司 双重内皮素受体拮抗剂与利尿剂的组合物
CN112679441A (zh) * 2019-10-18 2021-04-20 普济生物科技（台州）有限公司 阿普昔腾坦的晶型、制备方法及其用途
AU2020378025A1 (en) * 2019-11-07 2022-06-23 Crystal Pharmaceutical (Suzhou) Co., Ltd. Crystal form of Aprocitentan, preparation method therefor and use thereof
US20230167090A1 (en) 2020-05-21 2023-06-01 Teva Pharmaceuticals International Gmbh Solid state forms of aprocitentan and process for preparation thereof
US11730735B2 (en) 2020-07-10 2023-08-22 Astrazeneca Ab Combination of zibotentan and dapagliflozin for the treatment of endothelin related diseases
WO2023111797A1 (en) * 2021-12-17 2023-06-22 Janssen Biotech, Inc. Pyrimidine sulfamide derivatives and process for manufacturing them
EP4529461A1 (en) 2022-05-22 2025-04-02 Idorsia Pharmaceuticals Ltd Aprocitentan for the treatment of hypertension
WO2023227721A1 (en) 2022-05-25 2023-11-30 Idorsia Pharmaceuticals Ltd Crystalline forms of sodium (5-(4-bromophenyl)-6-(2-((5-bromopyrimidin-2-yl)oxy)ethoxy)pyrimidin-4-yl)(sulfamoyl)amide
WO2024140425A1 (zh) * 2022-12-30 2024-07-04 苏州科睿思制药有限公司 一种阿普昔腾坦晶型及其制备方法和用途

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002053557A1 (en) 2000-12-18 2002-07-11 Actelion Pharmaceuticals Ltd Novel sulfamides and their use as endothelin receptor antagonists
WO2003097045A1 (en) 2002-05-17 2003-11-27 Novartis Ag Combination of organic compounds
WO2007098390A2 (en) 2006-02-17 2007-08-30 Gilead Colorado, Inc. Method for treating resistant hypertension
WO2007146900A2 (en) 2006-06-15 2007-12-21 Gilead Colorado, Inc. Antihypertensive therapy method
WO2009026517A2 (en) 2007-08-22 2009-02-26 Gilead Colorado, Inc. Therapy for complications of diabetes
WO2009024906A1 (en) 2007-08-17 2009-02-26 Actelion Pharmaceuticals Ltd 4-pyrimidinesulfamide derivative
US8475839B2 (en) 2006-06-27 2013-07-02 Novartis Ag Solid dosage forms of valsartan, amlodipine and hydrochlorothiazide and method of making the same
WO2015121397A1 (en) 2014-02-14 2015-08-20 Actelion Pharmaceuticals Ltd Process for manufacturing pyrimidine sulfamide derivatives
WO2016073846A1 (en) 2014-11-07 2016-05-12 Abbvie Inc. Methods of treating ckd using predictors of fluid retention
WO2017185142A1 (en) 2016-04-29 2017-11-02 Adelaide Research & Innovation Pty Ltd Method for preventing and/or treating atrial fibrillation
WO2018154101A1 (en) 2017-02-27 2018-08-30 Idorsia Pharmaceuticals Ltd Crystalline forms of the 4-pyrimidinesulfamide derivative aprocitentan
WO2019106066A1 (en) 2017-11-30 2019-06-06 Idorsia Pharmaceuticals Ltd Combination of a 4-pyrimidinesulfamide derivative with an sglt-2 inhibitor for the treatment of endothelin related diseases

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT634175E (pt) * 1993-07-15 2001-06-29 Hoffmann La Roche Combinacao farmaceutica que contem um inibidor do sistema renina-angiotensina e o antagonista de endotelina
CN102614189B (zh) * 2012-04-17 2014-10-22 北京哈三联科技股份有限公司 含缬沙坦、氨氯地平和氢氯噻嗪的微丸药物组合
DK3897646T3 (da) * 2018-12-21 2024-07-01 Actelion Pharmaceuticals Ltd Macitentan til behandling af pulmonal arteriel hypertension

Patent Citations (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7285549B2 (en) 2000-12-18 2007-10-23 Actelion Pharmaceuticals Ltd. Sulfamides and their use as endothelin receptor antagonists
WO2002053557A1 (en) 2000-12-18 2002-07-11 Actelion Pharmaceuticals Ltd Novel sulfamides and their use as endothelin receptor antagonists
US7094781B2 (en) 2000-12-18 2006-08-22 Actelion Pharmaceuticals Ltd. Sulfamides and their use as endothelin receptor antagonists
US8101599B2 (en) 2002-05-17 2012-01-24 Novartis Ag Pharmaceutical composition containing anti-hypertensive agents
WO2003097045A1 (en) 2002-05-17 2003-11-27 Novartis Ag Combination of organic compounds
WO2007098390A2 (en) 2006-02-17 2007-08-30 Gilead Colorado, Inc. Method for treating resistant hypertension
WO2007146900A2 (en) 2006-06-15 2007-12-21 Gilead Colorado, Inc. Antihypertensive therapy method
US8475839B2 (en) 2006-06-27 2013-07-02 Novartis Ag Solid dosage forms of valsartan, amlodipine and hydrochlorothiazide and method of making the same
US8324232B2 (en) 2007-08-17 2012-12-04 Actelion Pharmaceuticals Ltd. 4-pyrimidinesulfamide derivative
US20120142716A1 (en) 2007-08-17 2012-06-07 Martin Bolli 4-pyrimidinesulfamide derivative
WO2009024906A1 (en) 2007-08-17 2009-02-26 Actelion Pharmaceuticals Ltd 4-pyrimidinesulfamide derivative
WO2009026517A2 (en) 2007-08-22 2009-02-26 Gilead Colorado, Inc. Therapy for complications of diabetes
WO2015121397A1 (en) 2014-02-14 2015-08-20 Actelion Pharmaceuticals Ltd Process for manufacturing pyrimidine sulfamide derivatives
US20160368882A1 (en) 2014-02-14 2016-12-22 Actelion Pharmaceuticals Ltd Process for manufacturing pyrimidine sulfamide derivatives
US9938244B2 (en) 2014-02-14 2018-04-10 Idorsia Pharmaceuticals Ltd Process for manufacturing pyrimidine sulfamide derivatives
WO2016073846A1 (en) 2014-11-07 2016-05-12 Abbvie Inc. Methods of treating ckd using predictors of fluid retention
WO2017185142A1 (en) 2016-04-29 2017-11-02 Adelaide Research & Innovation Pty Ltd Method for preventing and/or treating atrial fibrillation
WO2018154101A1 (en) 2017-02-27 2018-08-30 Idorsia Pharmaceuticals Ltd Crystalline forms of the 4-pyrimidinesulfamide derivative aprocitentan
WO2019106066A1 (en) 2017-11-30 2019-06-06 Idorsia Pharmaceuticals Ltd Combination of a 4-pyrimidinesulfamide derivative with an sglt-2 inhibitor for the treatment of endothelin related diseases

Non-Patent Citations (77)

* Cited by examiner, † Cited by third party
Title
"Characters Section in Monographs," European Pharmacopoeia 8.0, 5.11., 1 page.
Abstracts, Clinical Pharmacology & Therapeutics, vol. 103, Supp S1, p. S87 (2018).
Actelion Pharmaceuticals Ltd, "Actelion provides an update on the progress towards launching Idorsia—Key results for pipeline assets to be developed by Idorsia," Media Release, pp. 1-7 (2017).
Actelion Pharmaceuticals Ltd, "Actelion's Cardiovascular Pipeline Investor Webcast," Investor webcast, 52 pages (Nov. 7, 2016).
Atanur, S.S. et al, "The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance," Genome Research, vol. 20, pp. 791-803 (2010).
Aversa, M. et al, "Comparative Safety and Tolerability of Endothelin Receptor Antagonists in Pulmonary Arterial Hypertension," Drug Saf, 17 pages (2015).
Bakris, G.L. et al, "Divergent Results Using Clinic and Ambulatory Blood Pressures; Report of a Darusentan-Resistant Hypertension Trial," Hypertension, vol. 56, pp. 824-830 (2010).
Baltatu, O.C. et al, "Avosentan is protective in hypertensive nephropathy at doses not causing fluid retention," Pharmacological Research, pp. 1-5 (2013).
Bolli, M. H. et al, "The Discovery of N- [5-(4-Bromophenyl)-6-[2-[(5-bromo-2-pyrimidinyl)oxy]ethoxy]-4-pyrimidinyl- N′- propylsulfamide (Macitentan), an Orally Active, Potent Dual Endothelin Receptor Antagonist," Journal of Medicinal Chemistry, vol. 55, pp. 7849-7861 (2012).
Bolli, M. H. et al, "The Discovery of N-[5-(4-Bromophenyl)-6-[2-[(5-bromo-2-pyrimidinyl)oxy]ethoxy]-4-pyrimidinyl]-N′-propylsulfamide (Macitentan), an Orally Active, Potent Dual Endothelin Receptor Antagonist," Supporting Information, pp. 1-30.
Bolli, M.H., "The Discovery of Macitentan—A Standard Medicinal Chemistry Program?" Chimia, vol. 71(7/8), pp. 420-429 (2017).
Boss, C. et al, "From bosentan (Tracleer®) to macitentan (Opsumit®): The medicinal chemistry perspective," Bioorganic & Medicinal Chemistry Letters, vol. 26, pp. 3381-3394 (2016).
Bruderer, S. et al, "Absorption, distribution, metabolism, and excretion of macitentan, a dual endothelin receptor antagonist, in humans," Xenobiotica, pp. 1-10 (2012).
Burnier, "Update on Endothelin Receptor Antagonists in Hypertension," Current Hypertension Reports, vol. 20, No. 51, pp. 1-7, (2018); https://doi.org/10.1007/s11906-018-0848-0.
Burnier, M., "Update on Endothelin Receptor Antagonists in Hypertension," Current Hypertension Reports, vol. 20(51), pp. 1-7 (2018).
Calhoun, et al., "Triple Antihypertensive Therapy With Amlodipine, Valsartan, and Hydrochlorothiazide", Hypertension, vol. 54, p. 32-39, (2009).
Chow, C.K. et al, "Quarter-dose quadruple combination therapy for initial treatment of hypertension: placebo-controlled, crossover, randomised trial and systematic review," Lancet, vol. 389, pp. 1035-1042 (2017).
Danaietash et al., "Efficacy and safety of various doses of the new dual endothelin receptor antagonist aprocitentan in the treatment of hypertension," ESC Congress 2019 together with World Congress of Cardiology, Aug. 31-Sep. 4, 2019, Paris—France; 1 page.
Davenport, A.P. et al, "Endothelin," Pharmacological Reviews, vol. 68, pp. 357-418 (2016).
De Kanter, R. et al, "Physiologically-Based Pharmacokinetic Modeling of Macitentan: Prediction of Drug-Drug Interactions," Clin Pharmacokinet, 12 pages (2015).
Demir, D.B. et al, "New strategies to tackle diabetic kidney disease," Curr Opin Nephrol Hypertens, vol. 25(4), pp. 348-354 (2016).
Denolle, T. et al, "Management of resistant hypertension: expert consensus statement from the French Society of Hypertension, an affiliate of the French Society of Cardiology," Journal of Human Hypertension, vol. 30, pp. 657-663 (2016).
Egido, J. et al, "Atrasentan for the treatment of diabetic nephropathy," Expert Opinion on Investigational Drugs, 22 pages (2017).
Eirin, A. et al, "Emerging concepts for patients with treatment-resistant hypertension," Trends in Cardiovascular Medicine, pp. 1-7 (2016).
European Medicines Agency, "EMA/527460/2013 EMEA/H/C/001068; EPAR summary for the public; Exforge HCT; amlodipine / valsartan / hydrochlorothiazide," pp. 1-3 (2013).
Galiè, N. et al, "Seraphin haemodynamic substudy: the effect of the dual endothelin receptor antagonist macitentan on haemodynamic parameters and NT-proBNP levels and their association with disease progression in patients with pulmonary arterial hypertension," European Heart Journal, vol. 38, pp. 1147-1155 (2017).
Gavras, H. et al, "Malignant Hypertension Resulting from Deoxycorticosterone Acetate and Salt Excess; Role of Renin and Sodium in Vascular Changes," Circulation Research, vol. 36, pp. 300-309 (1975).
Goddard, J. et al, "Endothelin A Receptor Antagonism and Angiotensin-Converting Enzyme Inhibition Are Synergistic via an Endothelin B Receptor-Mediated and Nitric Oxide-Dependent Mechanism," Journal of the American Society of Nephrology, vol. 15, pp. 2601-2610 (2004).
Gradman, A.H. et al, "Combination therapy in hypertension," Journal of the American Society of Hypertension, vol. 4(1) pp. 42-50 (2010).
Griesser, U.J., "The Importance of Solvates," Chapter 8, Polymorphism in the Pharmaceutical Industry, pp. 211-233 (2006).
Gueneau De Mussy et al., "Effects of the Dual Endothelin Receptor Antagonist Aprocitentan on Body Weight and Fluid Homeostasis in Healthy Subjects on a High Sodium Diet," Clinical Pharmacology & Therapeutics, pp. 8, (2020).
Hunter, R.W. et al, "First-in-Man Demonstration of Direct Endothelin-Mediated Natriuresis and Diuresis," Hypertension, pp. 1-9 (2017).
Iglarz, M. et al, "Comparison of pharmacological activity of macitentan and bosentan in preclinical models of systemic and pulmonary hypertension," Life Sciences, vol. 118, pp. 333-339 (2014).
Iglarz, M. et al, "Pharmacology of Macitentan, an Orally Active Tissue-Targeting Dual Endothelin Receptor Antagonist," The Journal of Pharmacology and Experimental Therapeutics, vol. 327(3), pp. 736-745 (2008).
Iglarz, M. et al, "Vascular Effects of Endothelin Receptor Antagonists Depends on Their Selectivity for ETA Versus ETB Receptors and on the Functionality of Endothelial ETB Receptors," J Cardiovasc Pharmacol, vol. 66(4), pp. 332-337 (2015).
Janiak, P. et al, "Long-term blockade of angiotensin AT1 receptors increases survival of obese Zucker rats," European Journal of Pharmacology, vol. 534, pp. 271-279 (2006).
Khan, et al., "Real-life effectiveness, safety, and tolerability of amlodipine/valsartan or amlodipine/valsartan/hydrochlorothiazide single-pill combination in patients with hypertension from Pakistan", Therapeutic Advances in Cardiovascular Disease, vol. 8, Iss. 2, p. 45-55, (2014).
Kohan, D.E. et al, "Endothelin antagonists for diabetic and non-diabetic chronic kidney disease," British Journal of Clinical Pharmacology, vol. 76(4), pp. 573-579 (2012).
Kohan, D.E. et al, "Predictors of Atrasentan-Associated Fluid Retention and Change in Albuminuria in Patients with Diabetic Nephropathy," Clin J Am Soc Nephrol, vol. 10, pp. 1568-1574 (2015).
Laffin, L.J. et al, "Endothelin Antagonism and Hypertension: An Evolving Target," Seminars in Nephrology, vol. 35(2), pp. 168-175 (2015).
Lepist, E.I. et al, "Evaluation of the Endothelin Receptor Antagonists Ambrisentan, Bosentan, Macitentan, and Sitaxsentan as Hepatobiliary Transporter Inhibitors and Substrates in Sandwich-Cultured Human Hepatocytes," PLOS ONE, vol. 9(1), e87548, pp. 1-10 (2014).
Maguire, J.J. et al, "Endothelin Receptors and Their Antagonists," Seminars in Nephrology, vol. 35(2), pp. 125-136 (2015).
Mancia, G. et al, "2013 ESH/ESC Guidelines for the management of arterial hypertension; The Task Force for the management of arterial hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiology (ESC)," Journal of Hypertension, vol. 31(7), pp. 1281-1357 (2013).
Mann, J.F.E et al., "Avosentan for Overt Diabetic Nephropathy," J Am Soc Nephrol., vol. 21, No. 3, pp. 527-535, (2010).
Mann, J.F.E. et al, "Avosentan for Overt Diabetic Nephropathy," J Am Soc Nephrol., vol. 21(3), pp. 1-19 (2010).
Mccormack, T. et al, "Optimising hypertension treatment: NICE/BHS guideline implementation and audit for best practice," The British Journal of Cardiology, vol. 20 (Supplement 1):S1-S15 (2013).
Nielsen, E.A. et al, "Dual Endothelin Receptor Blockade Abrogates Right Ventricular Remodeling and Biventricular Fibrosis in Isolated Elevated Right Ventricular Afterload," PLOS ONE, pp. 1-18 (2016).
Rabelink, T.J. et al, "Endothelin Receptor Blockade in Patients with Diabetic Nephropathy," Contrib Nephrol., vol. 172, pp. 235-242 (2011).
Rapp, J.P, "Dahl Salt-Susceptible and Salt-Resistant Rats," Hypertension, vol. 4(6), pp. 753-763 (1982).
Remington, "Pharmaceutical Manufacturing," Part 5, The Science and Practice of Pharmacy, 21st Edition, 5 pages (2005).
Saleh, M.A. et al, "Distinct Actions of Endothelin A-Selective Versus Combined Endothelin A/B Receptor Antagonists in Early Diabetic Kidney Disease," The Journal of Pharmacology and Experimental Therapeutics, vol. 338(1), pp. 263-270 (2011).
Sen, S. et al, "Renal, retinal and cardiac changes in type 2 diabetes are attenuated by macitentan, a dual endothelin receptor antagonist," Life Sciences, pp. 1-11 (2012).
Sharma, K.H., "Did all thiazides take undue credit of good work of chlorthalidone?" Indian Journal of Pharmacology, vol. 48(5), 3 pages (2016).
Sidharta et al., "Single- and multiple-dose tolerability, safety, pharmacokinetics, and pharmacodynamics of the dual endothelin receptor antagonist aprocitentan in healthy adult and elderly subjects," Dove Medical Press journal: Drug Design, Development and Therapy, vol. 13, pp. 949-964, (2019).
Sidharta, P.N. et al, "Clinical Pharmacokinetics and Pharmacodynamics of the Endothelin Receptor Antagonist Macitentan," Clin Pharmacokinet, vol. 54, pp. 457-471 (2015).
Sidharta, P.N. et al, "Macitentan: entry-into-humans study with a new endothelin receptor antagonist," Eur J Clin Pharmacol, 8 pages (2011).
Sidharta, P.N. et al, "Pharmacokinetics of the Novel Dual Endothelin Receptor Antagonist Macitentan in Subjects With Hepatic or Renal Impairment," The Journal of Clinical Pharmacology, vol. 54(3), pp. 291-300 (2013).
The Fifteenth International Conference on Endothelin, ET-15, Program and Abstract Book, 2 pages (Oct. 4-7, 2017).
Thomson Reuters, "Actelion Ltd Cardiovascular Pipeline Update Corporate Call", Final Transcript, 17 pages (Nov. 7, 2016).
Treiber, A. et al, "Macitentan Does Not Interfere with Hepatic Bile Salt Transport," J Pharmacol Exp Ther, vol. 350, pp. 130-143 (2014).
Treiber, A. et al, "The metabolism of the dual endothelin receptor antagonist macitentan in rat and dog," Xenobiotica, pp. 1-15 (2015).
Trensz, F., "Pharmacological Characterization of Aprocitentan, a Dual Endothelin Receptor Antagonist, Alone and in Combination with Blockers of the Renin Angiotensin System, in Two Models of Experimental Hypertensions," J Pharmacol Exp Ther, vol. 368, pp. 462-473 (2019); Supplemental Figures, 6 pages.
Trensz, F., "Pharmacology of ACT-132577 (aprocitentan); A dual endothelin receptor antagonist for the treatment of resistant hypertension," ET-15 Conference, 19 pages (Oct. 5, 2017).
Tullos, N.A. et al, "Chronic blockade of endothelin A and B receptors using macitentan in experimental renovascular disease," Nephrol Dial Transplant, vol. 0, pp. 1-10 (2014).
U.S. Appl. No. 12/673,413, filed Dec. 4, 2012, Actelion Pharmaceuticals Ltd.
U.S. Appl. No. 15/118,046, filed Apr. 10, 2018, Idorsia Pharmaceuticals Ltd.
U.S. Appl. No. 16/489,227, filed Aug. 30, 2018, Idorsia Pharmaceuticals Ltd.
Valero-Munoz, M. et al, "Dual Endothelin-A/Endothelin-B Receptor Blockade and Cardiac Remodeling in Heart Failure With Preserved Ejection Fraction," Circ Heart Fail., pp. 1-9 (2016); Supplemental Material, 23 pages.
Vercauteren, M. et al, "Endothelin ETA Receptor Blockade, by Activating ETB Receptors, Increases Vascular Permeability and Induces Exaggerated Fluid Retentions," The Journal of Pharmacology And Experimental Therapeutics, vol. 361, pp. 322-333 (2017); Supplementary material, 2 pages.
Verweij et al., "Randomized Dose-Response Study of the New Dual Endothelin Receptor Antagonist Aprocitentan in Hypertension," Hypertension, vol. 75, pp. 1-10, (2020); DOI: 10.1161/Hypertensionaha.119.14504. 2 parts.
Wald, D.S. et al, "Combination Therapy Versus Monotherapy in Reducing Blood Pressure: Meta-analysis on 11,000 Participants from 42 Trials," The American Journal of Medicine, vol. 122(3), pp. 290-300, (2009).
Wan, X. et al, "A promising choice in hypertension treatment: Fixed-dose combinations," Asian Journal of Pharmaceutical Sciences, vol. 9, pp. 1-7 (2014).
Weber et al. (2009) 374:1423-31 The Lancet Pub. *
Weber, M.A. et al, "A selective endothelin-receptor antagonist to reduce blood pressure in patients with treatment-resistant hypertension: a randomised, double-blind, placebo-controlled trial," Lancet, vol. 374, pp. 1423-1431 (2009).
Weber, M.A. et al, "Clinical Practice Guidelines for the Management of Hypertension in the Community A Statement by the American Society of Hypertension and the International Society of Hypertension," The Journal of Clinical Hypertension, vol. 16(1), pp. 14-26 (2014).
Whelton, P.K. et al, "2017 High Blood Pressure Clinical Practice Guideline," Hypertension, 481 pages (2017).
Zhang, J. et al, "Pharmacokinetic study of ACT-132577 in rat plasma by ultra performance liquid chromatography-tandem mass spectrometry," Int J Clin Exp Med, vol. 8(10), pp. 18420-18426 (2015).

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11680058B2 (en) 2017-02-27 2023-06-20 Idorsia Pharmaceuticals Ltd Crystalline forms of a 4-pyrimidinesulfamide derivative aprocitentan
US11787782B2 (en) 2017-02-27 2023-10-17 Idorsia Pharmaceuticals Ltd Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases
US12144811B2 (en) 2017-11-30 2024-11-19 Idorsia Pharmaceuticals Ltd Combination of a 4-pyrimidinesulfamide derivative with an SGLT-2 inhibitor for the treatment of endothelin related diseases
US11464777B2 (en) 2018-12-21 2022-10-11 Actelion Pharmaceuticals Ltd Pharmaceutical composition for the treatment of pulmonary arterial hypertension
US11612600B2 (en) 2019-01-25 2023-03-28 Actelion Pharmaceuticals Ltd Pharmaceutical composition comprising macitentan for the treatment of chronic thromboembolic pulmonary hypertension

Also Published As

Publication number Publication date
IL315563A (en) 2024-11-01
SG10202111695RA (en) 2021-12-30
CN110325186A (zh) 2019-10-11
IL297993B1 (en) 2024-12-01
PT4014976T (pt) 2024-12-04
US20210206750A1 (en) 2021-07-08
MX2019010222A (es) 2019-10-24
CN110381948A (zh) 2019-10-25
US20230391757A1 (en) 2023-12-07
KR102577375B1 (ko) 2023-09-11
PH12019501937A1 (en) 2020-07-06
MA49664A (fr) 2020-06-03
US11787782B2 (en) 2023-10-17
IL297993B2 (en) 2025-04-01
MX392313B (es) 2025-03-21
TWI786089B (zh) 2022-12-11
JP7223701B2 (ja) 2023-02-16
KR20190121827A (ko) 2019-10-28
PL4014976T3 (pl) 2024-12-23
CN117946011A (zh) 2024-04-30
MA47596A (fr) 2021-05-05
LT4014976T (lt) 2024-11-11
JP2020508339A (ja) 2020-03-19
AU2018225309B2 (en) 2024-01-18
US10919881B2 (en) 2021-02-16
DK4014976T3 (da) 2024-12-02
IL268850B2 (en) 2025-02-01
UA126122C2 (uk) 2022-08-17
US20200061061A1 (en) 2020-02-27
EP3585391A1 (en) 2020-01-01
HRP20241461T1 (hr) 2025-01-03
RS66200B1 (sr) 2024-12-31
HUE069231T2 (hu) 2025-02-28
SG11201907435PA (en) 2019-09-27
MX2021007184A (es) 2021-07-21
AU2017400276A1 (en) 2019-10-17
IL268852A (en) 2019-10-31
KR102568472B1 (ko) 2023-08-18
JP2023027305A (ja) 2023-03-01
TWI854353B (zh) 2024-09-01
CA3053991A1 (en) 2018-08-30
MX2019010221A (es) 2019-10-21
CL2019002470A1 (es) 2020-02-21
AU2017400276B2 (en) 2024-01-11
SI4014976T1 (sl) 2025-01-31
CA3053994A1 (en) 2018-08-30
WO2018153513A1 (en) 2018-08-30
IL268850A (en) 2019-10-31
EP3658140A1 (en) 2020-06-03
EP4014976B1 (en) 2024-09-04
SG11201907604UA (en) 2019-09-27
PH12019501938A1 (en) 2020-07-06
BR112019017644A2 (pt) 2020-03-31
IL268850B1 (en) 2024-10-01
US11680058B2 (en) 2023-06-20
AU2018225309A1 (en) 2019-10-17
JP7520951B2 (ja) 2024-07-23
EP4014976A1 (en) 2022-06-22
CL2019002464A1 (es) 2020-01-31
ES3006308T3 (en) 2025-03-18
US20200002317A1 (en) 2020-01-02
IL297993A (en) 2023-01-01
TW201835071A (zh) 2018-10-01
WO2018154101A1 (en) 2018-08-30
US20220064149A1 (en) 2022-03-03
KR20190119635A (ko) 2019-10-22
KR20230074610A (ko) 2023-05-30
BR112019017658A2 (pt) 2020-03-31
FI4014976T3 (fi) 2024-11-05
TW202330502A (zh) 2023-08-01
JP2020508338A (ja) 2020-03-19
KR102700778B1 (ko) 2024-08-29
MY199557A (en) 2023-11-07
CL2020001762A1 (es) 2020-11-20

Similar Documents

Publication Publication Date Title
US11787782B2 (en) Combinations of a 4-pyrimidinesulfamide derivative with active ingredients for the treatment of endothelin related diseases
US12144811B2 (en) Combination of a 4-pyrimidinesulfamide derivative with an SGLT-2 inhibitor for the treatment of endothelin related diseases
EA043547B1 (ru) Фармацевтическая композиция, содержащая апроцитентан в комбинации с другими активными ингредиентами, применение апроцитентана во время лечения резистентной артериальной гипертензии в комбинации с другими активными ингредиентами

Legal Events

Date Code Title Description
FEPP Fee payment procedure

Free format text: ENTITY STATUS SET TO UNDISCOUNTED (ORIGINAL EVENT CODE: BIG.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

AS Assignment

Owner name: IDORSIA PHARMACEUTICALS LTD, SWITZERLAND

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ACTELION PHARMACEUTICALS LTD;REEL/FRAME:051471/0570

Effective date: 20190816

Owner name: ACTELION PHARMACEUTICALS LTD, SWITZERLAND

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:BELLET, MARC;BOLLI, MARTIN;CLOZEL, MARTINE;AND OTHERS;SIGNING DATES FROM 20190828 TO 20190829;REEL/FRAME:051471/0550

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: NOTICE OF ALLOWANCE MAILED -- APPLICATION RECEIVED IN OFFICE OF PUBLICATIONS

STPP Information on status: patent application and granting procedure in general

Free format text: PUBLICATIONS -- ISSUE FEE PAYMENT VERIFIED

STPP Information on status: patent application and granting procedure in general

Free format text: AWAITING TC RESP., ISSUE FEE NOT PAID

STPP Information on status: patent application and granting procedure in general

Free format text: PUBLICATIONS -- ISSUE FEE PAYMENT VERIFIED

STCF Information on status: patent grant

Free format text: PATENTED CASE